Genomic Map
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Target Gene Details
Entrez Gene ID: | 113402 |
Gene Name: | SFT2 domain containing 1 |
Gene Aliases: |
C6orf83, pRGR1 |
Location: |
Chr.6:166319728-166342606 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SFT2D1 | NM_145169.2 | NP_660152.1 | ||
| NR_130112.1 | ||||
| NR_130113.1 | ||||
| NR_130114.1 | ||||
| AF041429.1 | AAF18564.1 | |||
| AK021489.1 | 1 | 1223 | ||
| AL833217.1 | 1 | 2290 | ||
| AW964442.1 | ||||
| BC018969.1 | AAH18969.1 | |||
| BC028388.1 | 7 | 1573 | AAH28388.1 | |
| BF223532.1 | ||||
| BG706927.1 | ||||
| BI597156.1 |
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Additional Information:
For this assay, SNP(s) [rs576647603] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
non-DGV Variation
|
Gene Ontology Categories:
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